Canonical Allele Identifier: CA1008480779

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1647924693
• gnomAD v3: 1-162115805-G-A
• gnomAD v4: 1-162115805-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115805G>A , CM000663.2:g.162115805G>A	GRCh38
NC_000001.10:g.162085595G>A , CM000663.1:g.162085595G>A	GRCh37
NC_000001.9:g.160352219G>A	NCBI36
NG_015979.1:g.51015G>A
NG_015979.2:g.51015G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.106-38600G>A MANE Select	ENSP00000355133.5:n.106-38600G>A
ENST00000361897.9:c.106-38600G>A	ENSP00000355133.5:n.106-38600G>A
ENST00000430120.3:c.106-38600G>A	ENSP00000396713.3:n.106-38600G>A
ENST00000530878.5:c.106-38600G>A	ENSP00000431586.1:n.106-38600G>A
NM_001164757.1:c.106-38600G>A	NP_001158229.1:n.106-38600G>A
NM_014697.2:c.106-38600G>A	NP_055512.1:n.106-38600G>A
XR_922217.1:n.884-1903C>T
XR_922219.1:n.713-1903C>T
XR_922221.1:n.713-9057C>T
XR_002958375.1:n.3842-1903C>T
XR_002958378.1:n.3671-1903C>T
NM_014697.3:c.106-38600G>A MANE Select	NP_055512.1:n.106-38600G>A
NM_001164757.2:c.106-38600G>A	NP_001158229.1:n.106-38600G>A